Senior/Clinical Research Associate

IQVIA RDS PTY. LIMITED; North Sydney Council; On-site; AUD 95,000 - 149,000; Full time

Job summary

IQVIA Australia is hiring a Clinical Research Associate/Senior Clinical Research Associate. The role focuses on site monitoring, initiation, and close-out visits, and coordinating with sites to drive recruitment plans. You will manage multiple protocols, ensure regulatory submissions, and maintain study documentation.

Bachelor’s degree in Life Sciences is essential with at least 2 years’ independent monitoring experience. Travel interstate is required.

Qualifications

• Bachelor's degree is essential
• Minimum 2 years independent site monitoring experience
• Strong knowledge of GCP/ICH guidelines

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits and drive subject recruitment plans
• Provide monitoring visits and site management for multiple protocols and therapeutic areas
• Create and maintain documentation on monitoring findings and action plans, and liaise with study team

Job description

Job Type: Permanent position | Full time position

Job Description

IQVIA Australia Are you a Clinical Research Associate or Senior Clinical Research Associate looking for a new and exciting challenge with opportunity for ongoing support and growth? Are you looking for a career and not just a job?

Then we have the role for you! Key Responsibilities Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans

Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas Administer protocol and related study training to assigned sites and establish regular lines of communication Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations

Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans Collaborate and liaise with study team members for project execution support as appropriate.

Not everyone can be a CRA it’s an extraordinary role, do you meet this unique criteria? Bachelor's degree in Life Sciences or other scientific/nursing disciplines is essential Minimum of 2 years independent site monitoring experience

CRO experience is highly desired Ability to travel on a regular basis which will involve interstate travel Extensive knowledge of

Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is required $95,000 - $148,600 salary package + super https://www.iqvia.com/locations/australia-and-new-zealandthe way.